A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1155778



Internal ID22086283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:87146770..87274632hg38UCSC Ensembl
Outerchr2:87134049..87285720hg38UCSC Ensembl
Innerchr2:87373893..87501755hg19UCSC Ensembl
Outerchr2:87361172..87512843hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38151672
hg19151672
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4011365
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1155778
Frequency
Sample Size131
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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